About this role
Medpace will be hosting an In-Person Networking Event targeting Master's and PhD students in life sciences.
WHEN: May 7th at 5:00pm
**More details regarding the location of the event will be provided should you be selected to attend.
Responsibilities
Below are the positions we will be recruiting for at this event:
Associate Clinical Trial Manager (CTM)
- Compile and maintain project-specific status reports within the clinical trial management system;
- Interact with the internal project team, Sponsor, study sites, and third-party vendors;
- Provide oversight and quality control of our internal regulatory filing system;
- Provide oversight and management of study supplies;
- Create and maintain project timelines;
Clinical Data Coordinator:
- Validate entry database designs
- Report metrics and data trends on projects
- Identify data conflicts and issues on projects
- Work with personnel from global research sites to resolve data conflicts
Clinical Research Associate
- Comprehensive training program that provides resources and knowledge to monitor sites independently
- Travel to non-local, national study sites 60-80% of the time
- Communicate with medical staff and clinical research physicians on site
PK Analyst:
- Perform PK and PK/PD analyses (eg, NCA analysis)
- Collaborate with Biostatistician, Clinical Operations, Bioanalytical Scientist, and the Medical team for execution and management Phase I-III studies
- Present PK findings and represent Clincial Pharmacology in cross-functional study team settings.
Qualifications
- 3.3-3.5 GPA or higher
- Master's or PhD in Life Sciences or related fields
- Willing to work office-based in Cincinnati, OH
Medpace Overview
Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 6,000 people across 40+ countries.
Why Medpace?
People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.
The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.
Cincinnati Perks
- Cincinnati Campus Overview
- Flexible work environment
- Competitive PTO packages, starting at 20+ days
- Competitive compensation and benefits package
- Company-sponsored employee appreciation events
- Employee health and wellness initiatives
- Community involvement with local nonprofit organizations
- Discounts on local sports games, fitness gyms and attractions
- Modern, ecofriendly campus with an on-site fitness center
- Structured career paths with opportunities for professional growth
- Discounted tuition for UC online programs
Awards
Named a Top Workplace in 2024 by The Cincinnati Enquirer
- Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024
- Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility
What to Expect Next
A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.
About Medpace
Full-service contract research organization providing clinical development services across therapeutic areas. Headquartered in Cincinnati, OH.
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